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Expression of BRI2 mRNA and protein in normal human brain and familial British dementia: its relevance to the pathogenesis of disease
INTRODUCTION: Two different disease-specific mutations in the BRI2 gene, situated on chromosome 13, have been identified as giving rise to familial British dementia (FBD) and familial Danish dementia (FDD). Each mutation results in extension of the open reading frame generating the disease-specific...
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| 主要な著者: | , , , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2008
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| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2795351/ https://ncbi.nlm.nih.gov/pubmed/18282158 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2990.2008.00935.x |
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